Pill Identifier Omeprazole - NDC 0781-2790
Omeprazole
Product Code 0781-2790
Omeprazole by Sandoz Inc is a white capsule capsule delayed release about 18 mm in size, imprinted with ome;20. The product is a human prescription drug with active ingredient(s) omeprazole.
Omeprazole
Active Ingredient(s): Omeprazole
Inactive Ingredient(s):
- ANHYDROUS LACTOSE
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- MICROCRYSTALLINE CELLULOSE
- POVIDONE K25
- TALC
- MAGNESIUM OXIDE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- GELATIN, UNSPECIFIED
- TITANIUM DIOXIDE
- PROPYLENE GLYCOL
- SHELLAC
- POLYSORBATE 80
Sandoz Inc
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
0781-2790-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
0781-2790-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
0781-2790-31 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
0781-2790-92 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.